
Clinical Research Team Leader
Há 5 dias
As a Coordinator for Site Activation, you will execute tasks related to contract compliance and site startup activities in Brazil. Your role will involve collaborating with the Site Activation Manager, Project Management team, and other departments to ensure adherence to local and international regulations, standard operating procedures, project requirements, and contractual guidelines.
Essential Functions:- Perform site activation tasks according to applicable regulations, SOPs, and work instructions.
- Prepare site regulatory documents, reviewing for completeness and accuracy.
- Inform team members of completion of regulatory and contractual documents for individual sites.
- Distribute completed documents to sites and internal project team members.
- Support the updating and maintenance of internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project-specific information.
- Review, track, and follow up on the progress, approval, and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents.
- Bachelor's degree
- 1-3 years' experience in a similar position in a healthcare environment (site, CRO, pharma)
- At least 1 year managing contracts or managing start-up submissions
- Good interpersonal communication and organizational skills
- Advanced level of English
We are a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.
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